The fundamental relationships between the structure and properties of liquids are far from being well understood. For instance, the structural origins of many liquid anomalies still remain unclear, but liquid-liquid transitions (LLT) are believed to hold a key. However, experimental demonstrations of LLTs have been rather challenging. Here, we report experimental and theoretical evidence of a second-order-like LLT in molten tin, one which favors a percolating covalent bond network at high temperatures. The observed structural transition originates from the fluctuating metallic/covalent behavior of atomic bonding, and consequently a new paradigm of liquid structure emerges. The liquid structure, described in the form of a folded network, bridges two well-established structural models for disordered systems, i.e., the random packing of hard-spheres and a continuous random network, offering a large structural midground for liquids and glasses. Our findings provide an unparalleled physical picture of the atomic arrangement for a plethora of liquids, shedding light on the thermodynamic and dynamic anomalies of liquids but also entailing far-reaching implications for studying liquid polyamorphism and dynamical transitions in liquids.
Under uniaxial shock compression, the steepness of the plastic shock front usually exhibits power law characteristics with the Hugoniot pressure, also known as the “Swegle-Grady law.” In this Letter, we show that the Swegle-Grady law can be described better by a third power law rather than the classical fourth power law at the strain rate between . A simple dislocation-based continuum model is developed, which reproduced the third power law and revealed very good agreement with recent experiments of multiple types of metals quantitatively. New insights into this unusual macroscopic phenomenon are presented through quantifying the connection between the macroscopic mechanical response and the collective dynamics of dislocation assembles. It is found that the Swegle-Grady law results from the particular stress dependence of the plasticity behaviors, and that the difference between the third power scaling and the classical fourth power scaling results from different shock dissipative actions.